Canonical Allele Identifier: CA1932839527
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs1844145933

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835240_102835243dup , CM000672.2:g.102835240_102835243dup GRCh38
NC_000010.10:g.104594997_104595000dup , CM000672.1:g.104594997_104595000dup GRCh37
NC_000010.9:g.104584987_104584990dup NCBI36
NG_007955.1:g.7294_7297dup

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.436+14_436+17dup MANE Select ENSP00000358903.3:n.436+14_436+17dup
ENST00000638190.1:c.436+14_436+17dup ENSP00000492539.1:n.436+14_436+17dup
ENST00000638272.1:c.297+1825_297+1828dup ENSP00000491508.1:n.297+1825_297+1828dup
ENST00000638971.1:c.436+14_436+17dup ENSP00000492313.1:n.436+14_436+17dup
ENST00000639393.1:c.436+14_436+17dup ENSP00000492651.1:n.436+14_436+17dup
ENST00000640633.1:n.198+14_198+17dup
ENST00000369887.3:c.436+14_436+17dup ENSP00000358903.3:n.436+14_436+17dup
ENST00000489268.1:n.690+14_690+17dup
NM_000102.3:c.436+14_436+17dup NP_000093.1:n.436+14_436+17dup
NM_000102.4:c.436+14_436+17dup MANE Select NP_000093.1:n.436+14_436+17dup